A261 SEVERE ACUTE LIVER INJURY SECONDARY TO WILSON’S DISEASE: A CASE REPORT AND REVIEW OF THE LITERATURE

BACKGROUND: Wilson’s disease is autosomal recessive and rare (prevalence 1/30000-1/50000) caused by mutations in the ATP7B gene involved in copper excretion. Copper deposition drives hepatic injury, along with neuropsychiatric-ophthalmologic, and hematologic symptoms. Leipzig criteria greater than 4...

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Detalles Bibliográficos
Autores principales: Besney, J, Frolkis, A, McLellan, J, Congly, S, Nguyen, H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Poster Presentations
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991302/
http://dx.doi.org/10.1093/jcag/gwac036.261

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991302/
http://dx.doi.org/10.1093/jcag/gwac036.261

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